Volume 16, Number 14,
Issue of July 15, 1996
pp. 4389-4401
Copyright ©1996 Society for Neuroscience
The Behavior of Optic Axons on Substrate Gradients of Retinal
Basal Lamina Proteins and Merosin
Received Feb. 9, 1996; revised April 16, 1996; accepted April 23, 1996.
Willi Halfter
Department of Neurobiology, University of Pittsburgh, Pittsburgh,
Pennsylvania 15261
To study the behavior of optic axons to continuously changing
concentrations of their substrate, explants from embryonic retina were
placed across gradients of retinal basal lamina proteins and merosin.
The following growth patterns of axons in response to the substrate
gradients were found: (1) Axons that grew up gradients, i.e., from low
to high substrate concentrations, became longer and less fasciculated
with increasing concentration of the substrate. On shallow basal lamina
gradients, the axons also showed a directional response that resulted
in guidance to higher substrate concentrations. (2) Axons that grew
down gradients, i.e., from high to low substrate concentrations, became
shorter and more fasciculated with decreasing concentrations of the
substrate. On gradients of merosin, a significant alteration in the
axonal growth direction toward higher substrate concentrations was
detected. Axons heading down gradients never U turned to higher
substrate concentrations. (3) Axons confronted with discontinuous
substrates were confined to the borders of the substrate exclusively,
whereas axons confronted with substrate gradients were able to cross
into the territory beyond the substrate. (4) The growth patterns of
axons on substrate gradients of basal lamina proteins and merosin were
similar but not identical, indicating that axons may respond to
substrate gradients dependent on its chemical composition. The present
results show that substrate gradients can regulate length and
fasciculation of neurites and have a limited capability to direct axons
to higher substrate concentrations.
Key words:
axonal guidance;
substrate gradients;
optic
axons;
basal lamina;
extracellular matrix;
merosin